UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 515

Sortiert nach

Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies

Pharmacological reviews, 2018-01, Vol.70 (1), p.142-173

2018

Link zum Volltext

Verfügbarkeit prüfen

Molecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology

PLoS genetics, 2017-01, Vol.13 (1), p.e1006536-e1006536

2017

Link zum Volltext

Verfügbarkeit prüfen

SCN1A channelopathies: Navigating from genotype to neural circuit dysfunction

Frontiers in neurology, 2023-04, Vol.14, p.1173460-1173460

2023

Link zum Volltext

Verfügbarkeit prüfen

Biophysical characterization and modelling of SCN1A gain-of-function predicts interneuron hyperexcitability and a predisposition to network instability through homeostatic plasticity

Neurobiology of disease, 2023-04, Vol.179, p.106059-106059, Article 106059

2023

Link zum Volltext

Verfügbarkeit prüfen

Increased vulnerability of nigral dopamine neurons after expansion of their axonal arborization size through D2 dopamine receptor conditional knockout

PLoS genetics, 2019-08, Vol.15 (8), p.e1008352-e1008352

2019

Link zum Volltext

Verfügbarkeit prüfen

GDNF Overexpression from the Native Locus Reveals its Role in the Nigrostriatal Dopaminergic System Function

PLoS genetics, 2015-12, Vol.11 (12), p.e1005710-e1005710

2015

Link zum Volltext

Verfügbarkeit prüfen

Sodium channels and the neurobiology of epilepsy

Epilepsia (Copenhagen), 2012-11, Vol.53 (11), p.1849-1859

2012

Link zum Volltext

Verfügbarkeit prüfen

SCN1A gain of function in early infantile encephalopathy

Annals of neurology, 2019-04, Vol.85 (4), p.514-525

2019

Link zum Volltext

Verfügbarkeit prüfen

Non-Neurotoxic Nanodiamond Probes for Intraneuronal Temperature Mapping

ACS nano, 2017-12, Vol.11 (12), p.12077-12086

2017

Link zum Volltext

Verfügbarkeit prüfen

Quinidine in the treatment of KCNT1-positive epilepsies

Annals of neurology, 2015-12, Vol.78 (6), p.995-999

2015

Link zum Volltext

Verfügbarkeit prüfen

Global characterization of copy number variants in epilepsy patients from whole genome sequencing

PLoS genetics, 2018-04, Vol.14 (4), p.e1007285-e1007285

2018

Link zum Volltext

Verfügbarkeit prüfen

Interleukin-1 Receptor in Seizure Susceptibility after Traumatic Injury to the Pediatric Brain

The Journal of neuroscience, 2017-08, Vol.37 (33), p.7864-7877

2017

Link zum Volltext

Verfügbarkeit prüfen

Selective NaV1.1 activation rescues Dravet syndrome mice from seizures and premature death

Proceedings of the National Academy of Sciences - PNAS, 2018-08, Vol.115 (34), p.E8077-E8085

2018

Link zum Volltext

Verfügbarkeit prüfen

Electron paramagnetic resonance microscopy using spins in diamond under ambient conditions

Nature communications, 2017-09, Vol.8 (1), p.458-8, Article 458

2017

Link zum Volltext

Verfügbarkeit prüfen

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

Nature genetics, 2012-11, Vol.44 (11), p.1188-1190

2012

Link zum Volltext

Verfügbarkeit prüfen

KCNT1 gain of function in 2 epilepsy phenotypes is reversed by quinidine

Annals of neurology, 2014-04, Vol.75 (4), p.581-590

2014

Link zum Volltext

Verfügbarkeit prüfen

Established and emerging GABAA receptor pharmacotherapy for epilepsy

Frontiers in pharmacology, 2024-02, Vol.15, p.1341472-1341472

2024

Link zum Volltext

Verfügbarkeit prüfen

Hypothermia-induced dystonia and abnormal cerebellar activity in a mouse model with a single disease-mutation in the sodium-potassium pump

PLoS genetics, 2017-05, Vol.13 (5), p.e1006763-e1006763

2017

Link zum Volltext

Verfügbarkeit prüfen

Magneto-optical imaging of thin magnetic films using spins in diamond

Scientific reports, 2016-03, Vol.6 (1), p.22797-22797, Article 22797

2016

Link zum Volltext

Verfügbarkeit prüfen

GABA-mediated tonic inhibition differentially modulates gain in functional subtypes of cortical interneurons

Proceedings of the National Academy of Sciences - PNAS, 2020-02, Vol.117 (6), p.3192-3202

2020

Link zum Volltext

Verfügbarkeit prüfen

CRL4 antagonizes SCFFbxo7-mediated turnover of cereblon and BK channel to regulate learning and memory

PLoS genetics, 2018-01, Vol.14 (1), p.e1007165-e1007165

2018

Link zum Volltext

Verfügbarkeit prüfen

Sodium channel expression and transcript variation in the developing brain of human, Rhesus monkey, and mouse

Neurobiology of disease, 2022-03, Vol.164, p.105622-105622, Article 105622

2022

Link zum Volltext

Verfügbarkeit prüfen

Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy

PLoS genetics, 2017-03, Vol.13 (3), p.e1006684-e1006684

2017

Link zum Volltext

Verfügbarkeit prüfen

Histologic Analysis of Urethral Stricture in 9 Patients Following Dorsal Vaginal Graft Urethroplasty

American journal of clinical pathology, 2022-05, Vol.157 (5), p.742-747

2022

Link zum Volltext

Verfügbarkeit prüfen

The evaluation and treatment of nocturia: a consensus statement

BJU international, 2011-07, Vol.108 (1), p.6-21

2011

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 515

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(451)
Mit Volltextzugriff
(397)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies

Molecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology

SCN1A channelopathies: Navigating from genotype to neural circuit dysfunction

Biophysical characterization and modelling of SCN1A gain-of-function predicts interneuron hyperexcitability and a predisposition to network instability through homeostatic plasticity

Increased vulnerability of nigral dopamine neurons after expansion of their axonal arborization size through D2 dopamine receptor conditional knockout

GDNF Overexpression from the Native Locus Reveals its Role in the Nigrostriatal Dopaminergic System Function

Sodium channels and the neurobiology of epilepsy

SCN1A gain of function in early infantile encephalopathy

Non-Neurotoxic Nanodiamond Probes for Intraneuronal Temperature Mapping

Quinidine in the treatment of KCNT1-positive epilepsies

Global characterization of copy number variants in epilepsy patients from whole genome sequencing

Interleukin-1 Receptor in Seizure Susceptibility after Traumatic Injury to the Pediatric Brain

Selective NaV1.1 activation rescues Dravet syndrome mice from seizures and premature death

Electron paramagnetic resonance microscopy using spins in diamond under ambient conditions

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

KCNT1 gain of function in 2 epilepsy phenotypes is reversed by quinidine

Established and emerging GABAA receptor pharmacotherapy for epilepsy

Hypothermia-induced dystonia and abnormal cerebellar activity in a mouse model with a single disease-mutation in the sodium-potassium pump

Magneto-optical imaging of thin magnetic films using spins in diamond

GABA-mediated tonic inhibition differentially modulates gain in functional subtypes of cortical interneurons

CRL4 antagonizes SCFFbxo7-mediated turnover of cereblon and BK channel to regulate learning and memory

Sodium channel expression and transcript variation in the developing brain of human, Rhesus monkey, and mouse

Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy

Histologic Analysis of Urethral Stricture in 9 Patients Following Dorsal Vaginal Graft Urethroplasty

The evaluation and treatment of nocturia: a consensus statement

Suchergebnisse filtern